NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE49712 Query DataSets for GSE49712
Status Public on Aug 20, 2013
Title Comprehensive evaluation of differential gene expression analysis methods for RNA-seq data
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Third-party reanalysis
Summary A large number of computational methods have been recently developed for analyzing differential gene expression (DE) in RNA-seq data. We report on a comprehensive evaluation of the commonly used DE methods using the SEQC benchmark data set and data from ENCODE project. We evaluated a number of key features including: normalization, accuracy of DE detection and DE analysis when one condition has no detectable expression. We found significant differences among the methods. Furthermore, computational methods designed for DE detection from expression array data perform comparably to methods customized for RNA-seq. Most importantly, our results demonstrate that increasing the number of replicate samples significantly improves detection power over increased sequencing depth.
 
Overall design The Sequencing Quality Control Consortium generated two datasets from two reference RNA samples in order to evaluate transcriptome profiling by next-generation sequencing technology. Each sample contains one of the reference RNA source and a set of synthetic RNAs from the External RNA Control Consortium (ERCC) at known concentrations. Group A contains 5 replicates of the Strategene Universal Human Reference RNA (UHRR), which is composed of total RNA from 10 human cell lines, with 2% by volume of ERCC mix 1. Group B includes 5 replicate samples of the Ambion Human Brain Reference RNA (HBRR) with 2% by volume of ERCC mix 2. The ERCC spike-in control is a mixture of 92 synthetic polyadenylated oligonucleotides of 250-2000 nucleotides long that are meant to resemble human transcripts.
 
Contributor(s) Betel D, Mason CE, Zumbo P, Rapaport F, Khanin R, Pirun M, Krek A, Socci ND, Liang Y
Citation(s) 24020486
Submission date Aug 09, 2013
Last update date May 15, 2019
Contact name Doron Betel
Organization name Weill Cornell Medical College
Department Medicine
Street address 1305 York Avenue (Box 140)
City New York
State/province NY
ZIP/Postal code 10021
Country USA
 
Platforms (1)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
Samples (10)
GSM1206234 A replicate 1
GSM1206235 B replicate 1
GSM1206236 A replicate 2
This SubSeries is part of SuperSeries:
GSE47792 SEQC Project
Relations
Reanalysis of GSM958733
Reanalysis of GSM958748
Reanalysis of GSM958745
BioProject PRJNA214799
SRA SRP028705

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE49712_ENCODE_FPKM.txt.gz 781.0 Kb (ftp)(http) TXT
GSE49712_ENCODE_HTSeq.txt.gz 386.3 Kb (ftp)(http) TXT
GSE49712_HTSeq.txt.gz 443.1 Kb (ftp)(http) TXT
GSE49712_gene_FPKM.txt.gz 847.4 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Processed data are available on Series record
Raw data are available in SRA

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap